Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L63/00—Compositions of epoxy resins; Compositions of derivatives of epoxy resins
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
  • C08G63/66—Polyesters containing oxygen in the form of ether groups
  • C08G63/668—Polyesters containing oxygen in the form of ether groups derived from polycarboxylic acids and polyhydroxy compounds
  • C08G63/672—Dicarboxylic acids and dihydroxy compounds
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
  • C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
  • C08J5/04—Reinforcing macromolecular compounds with loose or coherent fibrous material
  • C08J5/06—Reinforcing macromolecular compounds with loose or coherent fibrous material using pretreated fibrous materials
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
  • Y10T428/2913—Rod, strand, filament or fiber
  • Y10T428/2933—Coated or with bond, impregnation or core
  • Y10T428/2964—Artificial fiber or filament
  • Y10T428/2967—Synthetic resin or polymer
  • Y10T428/2969—Polyamide, polyimide or polyester
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/31504—Composite [nonstructural laminate]
  • Y10T428/31511—Of epoxy ether
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T428/00—Stock material or miscellaneous articles
  • Y10T428/31504—Composite [nonstructural laminate]
  • Y10T428/31786—Of polyester [e.g., alkyd, etc.]
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
  • Y10T442/20—Coated or impregnated woven, knit, or nonwoven fabric which is not [a] associated with another preformed layer or fiber layer or, [b] with respect to woven and knit, characterized, respectively, by a particular or differential weave or knit, wherein the coating or impregnation is neither a foamed material nor a free metal or alloy layer
  • Y10T442/2311—Coating or impregnation is a lubricant or a surface friction reducing agent other than specified as improving the "hand" of the fabric or increasing the softness thereof
  • Y10T442/2328—Organosilicon containing
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
  • Y10T442/20—Coated or impregnated woven, knit, or nonwoven fabric which is not [a] associated with another preformed layer or fiber layer or, [b] with respect to woven and knit, characterized, respectively, by a particular or differential weave or knit, wherein the coating or impregnation is neither a foamed material nor a free metal or alloy layer
  • Y10T442/2311—Coating or impregnation is a lubricant or a surface friction reducing agent other than specified as improving the "hand" of the fabric or increasing the softness thereof
  • Y10T442/2336—Natural oil or wax containing
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
  • Y10T442/20—Coated or impregnated woven, knit, or nonwoven fabric which is not [a] associated with another preformed layer or fiber layer or, [b] with respect to woven and knit, characterized, respectively, by a particular or differential weave or knit, wherein the coating or impregnation is neither a foamed material nor a free metal or alloy layer
  • Y10T442/2738—Coating or impregnation intended to function as an adhesive to solid surfaces subsequently associated therewith
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
  • Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
  • Y10T442/20—Coated or impregnated woven, knit, or nonwoven fabric which is not [a] associated with another preformed layer or fiber layer or, [b] with respect to woven and knit, characterized, respectively, by a particular or differential weave or knit, wherein the coating or impregnation is neither a foamed material nor a free metal or alloy layer
  • Y10T442/2861—Coated or impregnated synthetic organic fiber fabric

Definitions

• polyester reinforcing articles such as filament, yarn, tire cord and the like, having improved adhesion when used as reinforcement in rubber articles are provided by cocrystallizingon the surface of a .conventional polyester reinforcing article a composition comprising a mixture comprising (1) a copolymer comprising crystallizable ester units identical to those present in the polyester reinforcing article, polyoxyalkylene groups and polyepoxy containing groups and (2) a polyepoxide.
• the surface modified polyester reinforcing articles are prepared by applying the treating composition to the poly ester article and subjecting the surface treated article to a temperature of at least 80 C. for a time suflicient to cause cocrystallization to take place on the surface of the treated polyester article.
• the polyester article is also treated, preferably by a second coating application, in a normal manner with a conventional polyhydric phenolaldehyde-rubber latex, and then bonded to rubber using conventional methods.
• Improved rubber articles reinforced with polyester reinforcing articles are obtained having outstanding adhesion between the rubber andthe polyester reinforcing articles.
• This invention relates to surface modified polyester reinforcing articles, such as filament, yarn, tire cord and the like, having outstanding adhesion to rubber when used in rubber reinforcing applications.
• polyester reinforcing elements such as polyethyle ene terephthalate filament or cord
• polyester reinforcing elements have physical characteristics, such as high strength,.fiex. resistance, high stretching modulus, low creep, and the like, which make. them outstanding materials for use in the reinforcement of rubber articles.
• serious. problems affect the use of polyester reinforcing elements in rubber .reinforce ment applications due to the very .poor rubber. adhesion properties associated with polyester articles.
• aqueous dispersions contaimng a combina tion of a resorcinol-formaldehyde condensateand-a-vinyL pyridine latex (referred to as a RFL dip) is best known as an effective treating agent for improving the rubber adhesion ofsome synthetic polymer reinforcing elements, such as nylon reinforcing elements.
• RFL dips do not satisfactorily overcome the problems encoun tered with polyester reinforcing element adhesion. Therefore, attempts have been made to either find new treating agents for improving the rubber adhesion of polyester reinforcing elements or to treat the polyester with additional agents in combination with the RFL dip treatment to improve the adhesion.
• Another object of this invention is to provide surface modified polyester articles to which can be applied a coating of a polyhydric phenol-aldehyde-rubber latex treating agent, such as resorcinol-formaldehyde-vinyl pyridine latex, to provide outstanding rubber adhesion properties to the treated surface modified polyester articles.
• a polyhydric phenol-aldehyde-rubber latex treating agent such as resorcinol-formaldehyde-vinyl pyridine latex
• Another object of this invention is to provide improved rubber adhesion to polyester articles by a method which is convenient and carried out in combination with conventional processing steps.
• the objects of this invention are accomplished and p the disadvantages found in prior art practices are overcome by providing surface modified polyester articles having improved adhesion when used as reinforcing elements in rubber articles by cocrystallizing on the surface of a conventional polyester article a composition comprising a mixture comprising (1) from about 10-to 50 percent by weight of a polymer comprising from about 15 to 30 .percent by weight of crystallizable ester units identical to those present in the polyester article, from about '60 to 80 percent by weight of polyoxyalkylene groups and from about 1 to 25 percent by weight of polyepoxy containing groups and (2) from about 15 to 60 percent by weight of a polyepoxide.
• the treating composition may contain from about 10 to 50 percent by weight of a textile lubricant.
• the surface modified polyester articles are prepared by applying the treating composition to the surface of the polyester article and subjecting the surface treated article to a temperature of at least 80 C. for a time sufficient to cause cocrystallization to take place on the surface of-the treated polyester article.
• polyester articles treated in accordance with this invention are composed of polyesters which are conventional and well known to those skilled in the art.
• Illustrative' of the polyesters useful in preparing shaped structures, such as filaments, fibers, threads, yarn, cords, fabrics, webs, and the like, which may be treated in accordance with this invention and are thereafter useful in rubber-reinforcement applications are those disclosed in US. Pats. Nos. 2,465,319, No. 2,965,613 and-No. 2,901,466.
• Polyethylene terephthalate is preferred for use as the reinforcing articles of this invention.
• Polyethylene terephthalate is obtained by reacting terephthalic acid or dimethyl terephthalate with ethylene glycol under conventional polyester forming conditions-The resulting polymer is then extruded or shaped into the desired article by conventional techniques.
• the treating composition critical for the purposes of this invention is composed of (l) a polymer comprised of ester units which are repeat units identical with those forming the crystallizable portions of the polyester article being treated, polyoxyalkylene groups sufficient to render the surface of the polyester article hydrophilic and therefore wettable by water, and polyepoxy containing groups as defined hereafter and (2) a polyepoxide as defined here after.
• the treating composition will also 'contain a lubricating finish which has been found to greatly aid the processing of the treated article in addition to giving improved adhesion properties.
• the polymer which is a part of the treating composition should be present in the treating composition in amounts of from about to 50 percent byweight and is comprised of from about to 30 percent by weight of ester units, from about 60 to 80 percent by Weight of polyoxyalkylene groups and from about 1 to percent by weight of polyepoxy containing groups.
• the polymer will be present in the treating composition in amounts of from about 25 to percent by weight and be composed of from about 20 to 25 percent by weight of ester units, from about 65 to 75 percent by weight of polyoxyalkylene groups, and from about "5, to 10 percent by weight of polyepoxy containinggroups.
• ester units which are a critical part of the polymer are identical with the crystallizable repeat units found in the polyester article to be treated and are believed to cocrystallize with those identical units in the polyester in order to fix the treating composition to the polyester article.
• polyester article to be treated is com; posed of polyethylene terephthalate as preferred, the
• polyoxy-' alkylene groups for the purposes of the present invention include polyoxymethylene, polyoxyethylne, p'olyoxy- P py p y y y and the like- Pfefefilblyfthd of the polymer useful for the purposes of this invention polyoxyalkylene groups will be polyoxyethylene' groupsi
• the polyepoxy containing groups which are a criticalpart of the polymer are derived from a polye'poxidahav ing one or more epoxy groups.
• the epoxygroup may be present in an amount greater than 0.20 equivalent per 100 grams of epoxy material as determined'by standard analysis and preferably has a molecular weight below about 9 00 and may be saturated or unsaturatedand aliphatic, cycloaliphatic and aromatic, andrnay be substituted with such radicals as chlorine, hydroxy, alkoxy, and the like.
• the polyepoxides from which the epoxy radicals are derived are described in detailjhe'reafterl
• the treating composition also contains a polyepoxide epoxide having one or more epoxy groups.
• the epoxy group may'be present in an amount greater than 0.02
• epoxy material as deter mined by standard analysis and preferably has a molecular weight below about 900 and may be saturated or unsaturated and aliphatic, cycloaliphatic and aromatic, and my be substituted with such radicals as chlorine, hydroxy, alkoxy, and thelike.
• Polyepoxide compositions suitable for the purposes of this invention are well known to those skilled in theart and are described in numerous references such as US. Pat. No.'2,902,398.
• Polyglycidic ethers of polyhydric aliphatic alcohols in which there are at least three hydroxy groups, at least two of these hydroxy groups being replaced by the glycidyl ether radical are preferred for use in the treating compositions of this invention, both as an ingredient in the polymer which forms a part of the treating composition and as a separate ingredient of the treating composition
• Polyglycidic ethers of thistype may be represented by the following structural formula wherein R represents a straight or branched chain alkylone group having up to 10 carbon atoms, preferably 3 to 6 carbon atoms,
• R represents hydrogen or the glycidic radical well known and is described in detail in the preparation of polyether A at column 4 of US. Pat. No. 2,902,398.
• the treating composition may also contain from about 10 to-50 percent by weight of a textilel'ubricant and preferably from about .20 to30percent by weight of the lubricant.
• the inclusion of atextile lubricant in the treating composition aids in the later processing of the treated article into many reinforcing applications.
• Suitable textile lubricants are those well known in the art,
• amineral or vegetable oil as, for example, a light mineral oil, olive oil, sperm oil, or a processed oil such as a sulfonated castor oil, or a synthetic material such as a 'silicone oil.
• the polymers which form a critical part of the treating composition are conveniently prepared by reacting the esterfo'rming reactants,'such as ethylene glycol and terephthalic acid or ester forming derivatives thereof, a polyoxyalkylene glycol, and a polyepoxide under conventional esterification and polymerization techniques.
• the viscosity should range fromv above 0.3 to below 0.55 and, preferably willrange from about 0.4'to 0.5 as measured in a 0.4 per cent solution in triflnoroacetic acid at 30 C.
• thetreating composition be crystallizable.
• the treating composition may be applied tothe polyester article as a molten material, as a solution in alplast'icizer for thepolyester being treated, as a solutionin' a solvent which does not plasticize the polyester being treated, oras a suspension or,dispersion of the treating composition in a .liquid m'edium.
• a preferred method of applying the treating composition is from a dispersion in water "or aqueous medium.
• a temperature of above 80 C. is required to produce a durable surface treatment.
• a heat treatment in the range of from about 80 C. to just below the melting point of the polyester article being treated for a time sufficient to cause cocrystallization to take place between the ester units of the treating composition and the polyester being treated has been found to be satisfactory. It has been found that a heat treatment at a temperature of about 100 to 220 C. for a period of from about 0.5 second to 2 minutes provides very satisfactory results.
• the treating composition should be applied to the surface of the polyester article so that from about 0.3 to 1.5 percent by weight solids are present on the surface of the polyester.
• a preferred procedure for the preparation of the surface modified polyester articles of this invention involves dispersing the polymer comprising about 20 to 25 percent by weight of the ester units, about 65 to 75 percent by weight of the polyoxyalkylene groups, and about 5 to percent by weight of the polyepoxy containing groups in water at about 40 to 60 C. to provide about a 10 to 30 percent by weight solids dispersion.
• To this dispersion sufficient amounts of the polyepoxide and, preferably, a textile lubricant are added to provide a dispersion of about 23 to 25 percent by weight solids comprising about 20 to 40 percent by weight of the polymer, about 30 to 60 percent by weight of the polyepoxide, and about 20 to 30 percent by weight of the textile lubricant.
• This dispersion is applied to the surface of the polyester article, preferably in filament form, and the treated article is then heated at a temperature of about 135 C. for about 5 seconds to attain a durable coating of the treating composition upon the article in the amount of about 0.9 percent by weight solids on the surface of the article.
• the treatment of this invention does not affect the polyester article in such a way and the article remains quite flexible. Therefore, the treatment of the polyester article may be carried out at any time after the initial shaping of the polyester reinforcing article, e.g., before or after filaments have been formed into threads, yarns, cords, fabrics or the like.
• the heat fixed base coating comprising the polymer comprising the esterunits, polyoxyalkylene units, and epoxy units and the polyepoxide is applied to the article and simultaneously therewith or preferably thereafter a second coating comprising a known polyhydric alcohol-aldehyde-latex bonding agent is applied in a known manner.
• compositions produced according to the present invention may be utilized for a Wide variety of important industrial applications. They are of particular value in the preparation of pneumatic tires for automobiles, tractors, busses, aircraft, and the like as well as in the preparation of conveyor belts, hoses, transmission belts, raincoats, and the like. 1
• the surface modified polyester articles of this invention are normally treated with the polyhydric alcohol-aldehydelatex adhesive mixture before the article is bonded to rubber.
• These polyhydric alcohol-aldehyde-latex adhesivemixtures are well known and conventional, to the art.;
• the surface modified polyester articles are. given a second coating of a composition containing a resorcinolformaldehyde condensate and a butadiene-styrene-vinylpyridine latex to provide about 4 to 8 percent by welght solids on the surface ofthe polyester article.
• the resor-' cinol-formaldehyde-latex composition may also contain other known adhesive additives such as a blocked diisocyanate if so desired.
• the polyester article is then bonded to rubber to provide products for a wide variety of important industrial applications.
• the final product is of particular value in pneumatic tires for automobiles, busses, tractors, aircraft, and the like.
• the bonding of the reinforcing article to the rubber in the final product is accomplished by conventional and well known techniques.
• the nature of the rubber in the final reinforced shaped structure is not critical. It may be either a natural or a synthetic rubber.
• the rubber stock used may contain conventional additives, such as stabilizers, vulcanizers, antioxidants, fillers, pigments and the like, if desired.
• the polyester tire cord used in the examples is prepared using conventional methods.
• Polyethylene terephthalate is prepared from dimethyl terephthalate and ethylene glycol and melt spun into filaments which are combined into yarn.
• the adhesion treatments of the examples are applied to the yarn and the treated yarn is drawn and then processed into tire cord consisting of 3 plies having 98 twist and 9Z twist.
• the tire cord is subjected to a conventional H-Block test in which the treated cord is cured across the center of two small inch width) rectangles of rubber with a short length of the cord between the rubber pieces forming the crossbar of the H.
• the pieces of rubber are gripped in an Instron Tensile Testing Machine and stress is applied so that the cord is pulled out from one of the pieces of rubber.
• the load required is regarded as a measure of the adhesion.
• the polymers which form a critical part of the treating compositions of this invention and used in the examples which follow may be prepared as follows: The necessary quantities of dimethyl terephthalate, ethylene glycol, polyoxyethylene glycol having an average molecular weight of 4000 and the polyglycidic ether as prepared below are heated at 165 C. Until the theoretical amount of methanol is distilled off. The mixture is then slowly heated to 220 C. to drive off any remaining methanol. A small amount (0.1%) of antimony trioxide catalyst is added to the reaction mixture and the mixture is polymerized at a temperature of about 275 C. and under a vacuum of 2 mm. for a period of about 1 hours to obtain a polymer having an intrinsic viscosity of about 0.4 to 0.5.
• the polyglycidyl ether used throughout the examples is the reaction product of epichlorohydrin and glycerol and may be prepared as follows: About 276 parts (3 moles) of glycerol is mixed with 832 parts (9 moles) of epichlorohydrin. To this reaction mixture is added 10 parts of diethyl ether solution containing about 4.5 percent boron tritiuoride. The temperature of this mixture is kept between 50 C. and 75 C. for about 3 hours. About 370 parts of the resulting glycerol-epichlorohydrin condensate is dissolved in 900 parts of dioxane containing about 300 parts of sodium aluminate. With agitation, the reaction mixture is heated and refluxed at 93 C.
• RFL adhesive mixture was prepared as follows: Eleven parts by weight of resorcinol, 16.2 parts by weight of 37% formaldehyde, 0.3 part by weight of. sodium hydroxide, and 238.5 parts by weight of water were mixed, aged for six hours at 75-78 F. and then added to a mixture of 244 parts by weight of 41% solids, butadiene-styrene-vinylpyridine polymer latex (70:15:15) diluted with 60 parts by weight of water. I
• the RFL mixture was applied to the polyethylene terephthalate yarn to provide a dry solids pick-up of about 4.5 percent by weight.
• the yarn was processed into tire cord and the treated cord was cured at about 430 F. for about one minute, then bonded to rubber stock and then tested for adhesion using the H-Block test. A value set at 100 was obtained.
• EXAMPLE 2 A polymer having an intrinsic viscosity of 0.45 and comprising about 22 perecnt by weight of ethylene terephthalate units, about 71 perecnt by weight of polyoxyethylene groups which have been derived from a polyoxyethylene glycol of an average molecular weight of about 4000, and about 7 percent by weight of a polyglycidic ether co mponent derived from the reaction product of glycerol and epichlorohydrin is dispersed in water at about 40 to 60 C. to provide about a 20 percent by weight solids dispersion.
• This dispersion was applied to the polyethylene terephthalate yarn and the yarn was heated at about 135 C. for about seconds to atttain a durable coating of the treat-. ing composition upon the article in the amount of about 0.9 percent by weight solids on the surface of the article.
• the treated yarn was then coated with the RFL mixture as described in Example 1, processed into tire cord, bonded to rubber stock, and tested for adhesion using the H-Block test. An adhesion rating of 326 as compared to a rating of 100 for the control was obtained. 1
• EXAMPLE 3 A suspension of about 5 percent by weightsolids'comprising about 72 percent by weight of a phenol blocked" methylene-bis-(4-phenylisocyanate), about 27 percent by weight of the polyglycidic ether obtained by the'reaction of glycerol and epichlorohydrin and about 1 percent by weight of a natural gum was applied to a polyethylene terephthalate yarn and then dried at about 440,F. tor about 1 minute. p e
• the treated yarn was then coated with the mixture as described in Example 1, processed into tire cord, bonded to rubber stock, and tested for adhesion usingthe H-Block test. An adhesion rating of 246 was obtained.
• EXAMPLE 4 Polyethylene terephthalate yarn was precoat'ed with the composition of this invention as described in" Example 2 and then subjected to the treatment as described'in Exani ple 3. An adhesion rating of 366 was obtained as 'corn-' pared to a rating of 246 for the commercial treatment as represented by Example 3.
• EXAMPLE 5 A suspension of about 20 percent by weight solids comprising 77 percent by weight of the RFL mixture as described in Example 2 and about 23 percent by weight of H7 adhesive additive was applied to a polyethylene terephthalate yarn and then dried at about 450 C.- forab,o,ut1
• H7 adhesive additive is a commercially available additive for polyester rubber adhesionsold by I.C.I. Organics, Inc. of Stamford, Conn. and is a solution of a complex phenolic based compound in dilute ammonia?
• the treated yarn was. then processed into tire cord, bonded to rubber stock, and tested for adhesion using the H-Block test. An adhesion rating of 334 was obtained.
• EXAMPLE 6 Polyethylene terephthalate yarn was precoatcd with the composition of this invention as described in Example 2 and then subjected to the treatment as described in Example 5. An adhesion rating of 464 was obtained as compared to a rating of 334 for the commercial treatment as represented by Example 5.
• EXAMPLE 7 Polyethylene terephthalate yarn was treated as described in Example 2 except that the precoating dispersion comprised only the polymer and did not contain the polyepoxide or the textile lubricant.
• compositions comprising a mixture comprising (1) about '10 to 50 percent j iby weight of a copolymer comprising about 15 to 30 percent'byiweight of ester units identical to those presentin the polyester, about 60 to '80 percent by weight of. polyoxyalkylene groups, and about 1 to 25 percent by weight o fi polyepoxy containing groups derived from a polyepoxide having. atlleastone epoxy group and (2) about ,15 to 60 percent, by weight of a polyepoxide, said polyepoxide beingidentical to, the polyepoxide used in the preparation. of said copolymer.
• a surface modified polyester article as-defined in claim l'wherein said mixture also contains from about 10 to 50 percent byweight of a textile-lubricating agent.
• polyester is comprised of polyethylene' terephthalate, the copolymer iscomprised of ethylene terephthalate units, polyoxyethylene groups having an avera'g e 'molecula r"weight of about 1500'to 6000, and a polyglycidic ether radical derived from the reaction product ofepichlorohydrin and glycerol and the polyepoxideis comprised of the polyglycidyl ether which is the reaction product of epichlorohydrin and glycerol.

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• Chemical & Material Sciences (AREA)
• Health & Medical Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Medicinal Chemistry (AREA)
• Polymers & Plastics (AREA)
• Organic Chemistry (AREA)
• Engineering & Computer Science (AREA)
• Materials Engineering (AREA)
• Manufacturing & Machinery (AREA)
• Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

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Family Applications (1)

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Cited By (1)

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• 1971
  • 1971-06-03 US US00149822A patent/US3729336A/en not_active Expired - Lifetime
• 1972
  • 1972-04-13 CA CA139,646A patent/CA975486A/en not_active Expired
  • 1972-04-14 GB GB1729972A patent/GB1399656A/en not_active Expired
  • 1972-05-12 BE BE783342A patent/BE783342A/xx unknown
  • 1972-05-12 FR FR7217098A patent/FR2139879B1/fr not_active Expired
  • 1972-05-13 IT IT50224/72A patent/IT957837B/it active
  • 1972-05-25 JP JP5131472A patent/JPS5342840B1/ja active Pending

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